LRRC7, leucine rich repeat containing 7, 57554

N. diseases: 26; N. variants: 6
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12062605
rs12062605
0.925 0.040 1 69995152 intron variant T/C snv 6.0E-02
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs12062605
rs12062605
0.925 0.040 1 69995152 intron variant T/C snv 6.0E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs1418004
rs1418004
1 69651765 intron variant C/T snv 0.36
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs17131023
rs17131023
1.000 0.080 1 69753508 intron variant T/C snv 3.5E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs2226284
rs2226284
1 69869999 intron variant T/C;G snv 0.47
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.700 1.000 1 2012 2012
dbSNP: rs687531
rs687531
1 70059551 intron variant C/T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability
0.700 1.000 1 2018 2018
dbSNP: rs672961
rs672961
1.000 0.040 1 70101505 intron variant C/G snv 0.99
Respiratory Distress Syndrome, Adult
Respiratory Tract Diseases 0.010 1.000 1 2015 2015